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      Pd-N-heterocyclic carbene catalyzed synthesis of piperidine alkene-alkaloids and their anti-cancer evaluation.

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          Abstract

          A facile synthesis of piperidine alkene-alkaloids including natural (+)-Caulophyllumine B in high yields has been developed by Heck cross-coupling reaction catalyzed by simple in situ formed palladium-N-heterocyclic carbenes (Pd-NHCs). Formation of Pd(0) nanoparticles has been noticed during the reaction course. The synthesized piperidine alkene-alkaloids were evaluated for in vitro anti-cancer activity against a panel of human tumor cell lines of lung, breast and ovarian. Several of these piperidine alkene-alkaloids were found to possess highest growth inhibition activity than the standard drug cisplatin and support the concept to modulate drug receptor interaction.

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          Author and article information

          Journal
          Bioorg. Med. Chem. Lett.
          Bioorganic & medicinal chemistry letters
          Elsevier BV
          1464-3405
          0960-894X
          Feb 15 2014
          : 24
          : 4
          Affiliations
          [1 ] Department of Chemistry, Kakatiya University, Warangal, India. Electronic address: shravankankala@yahoo.com.
          [2 ] Institute of Biotechnology, National Dong-Hwa University, Shou-Feng, Hualien 974, Taiwan, ROC.
          [3 ] Department of Chemistry, Satavahana University, Karimnagar, India.
          [4 ] Department of Chemistry, Kakatiya University, Warangal, India.
          Article
          S0960-894X(13)01492-3
          10.1016/j.bmcl.2013.12.108
          24447851
          55a38999-b150-4eae-a4a6-427f0d8ec426
          History

          N-Heterocyclic carbene,Heck coupling,Anti-cancer activity,Piperidine alkene–alkaloids,Natural products

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